OneTouch Delica Safety OTD Safety 30g US 200

GUDID 20812608030266

Box of 200 Sterile Single-Use Lancing Device 30 Gauge

ASAHI POLYSLIDER COMPANY,LIMITED

Manual blood lancing device, single-use

• Primary Device ID: 20812608030266
• NIH Device Record Key: acdfc3cc-2e6f-413d-92bf-82b878320398
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OneTouch Delica Safety
• Version Model Number: 024-318
• Catalog Number: OTD Safety 30g US 200
• Company DUNS: 718296825
• Company Name: ASAHI POLYSLIDER COMPANY,LIMITED
• Device Count: 200
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 1 888 567-3003
• Email: customerservice@lifescan.com
• Phone: 1 888 567-3003
• Email: customerservice@lifescan.com
• Phone: 1 888 567-3003
• Email: customerservice@lifescan.com
• Phone: 1 888 567-3003
• Email: customerservice@lifescan.com
• Phone: 1 888 567-3003
• Email: customerservice@lifescan.com
• Phone: 1 888 567-3003
• Email: customerservice@lifescan.com
• Phone: 1 888 567-3003
• Email: customerservice@lifescan.com
• Phone: 1 888 567-3003
• Email: customerservice@lifescan.com
• Phone: 1 888 567-3003
• Email: customerservice@lifescan.com
• Phone: 1 888 567-3003
• Email: customerservice@lifescan.com

Device Dimensions

• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge
• Needle Gauge: 30 Gauge

Device Identifiers

Device Issuing Agency	Device ID
GS1	00812608030262 [Primary]
GS1	20812608030266 [Package]; Contains: 00812608030262; Package: Cardboard box [24 Units]; In Commercial Distribution
GS1	80812608030244 [Unit of Use]

FDA Product Code

• FMK: Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-12-05
• Device Publish Date: 2022-11-25

On-Brand Devices [OneTouch Delica Safety]

• 00812608030255: Box of 200 Sterile Single-Use Lancing Device 23 Gauge
• 20812608030228: Box of 200 Sterile Single-Use Lancing Device 30Gauge
• 20812608030266: Box of 200 Sterile Single-Use Lancing Device 30 Gauge